Canonical Allele Identifier: CA2549809157

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23630347_23630348insCCC , CM000678.2:g.23630347_23630348insCCC	GRCh38
NC_000016.9:g.23641668_23641669insCCC , CM000678.1:g.23641668_23641669insCCC	GRCh37
NC_000016.8:g.23549169_23549170insCCC	NCBI36
NG_007406.1:g.16010_16011insGGG , LRG_308:g.16010_16011insGGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.1812_1813insGGG	ENSP00000460666.3:p.Gln604_Leu605insGly
ENST00000565038.2:c.212-1073_212-1072insGGG	ENSP00000459882.2:n.212-1073_212-1072insG...
ENST00000566069.6:c.1806_1807insGGG	ENSP00000459237.2:p.Gln602_Leu603insGly
ENST00000697377.2:c.1812_1813insGGG	ENSP00000513286.2:p.Gln604_Leu605insGly
ENST00000697379.2:c.1812_1813insGGG	ENSP00000513287.2:p.Gln604_Leu605insGly
ENST00000561514.2:c.921_922insGGG	ENSP00000460666.2:p.Gln307_Leu308insGly
ENST00000697374.1:c.921_922insGGG	ENSP00000513284.1:p.Gln307_Leu308insGly
ENST00000697375.1:n.3153_3154insGGG
ENST00000697376.1:c.921_922insGGG	ENSP00000513285.1:p.Gln307_Leu308insGly
ENST00000697377.1:c.921_922insGGG	ENSP00000513286.1:p.Gln307_Leu308insGly
ENST00000697378.1:n.2326_2327insGGG
ENST00000697379.1:c.921_922insGGG	ENSP00000513287.1:p.Gln307_Leu308insGly
ENST00000697380.1:n.734_735insGGG
ENST00000697381.1:n.501_502insGGG
ENST00000697382.1:c.921_922insGGG	ENSP00000513288.1:p.Gln307_Leu308insGly
ENST00000697383.1:c.49-1073_49-1072insGGG	ENSP00000513289.1:n.49-1073_49-1072insGGG...
ENST00000697384.1:n.1960_1961insGGG
ENST00000261584.9:c.1806_1807insGGG MANE Select	ENSP00000261584.4:p.Gln602_Leu603insGly
ENST00000261584.8:c.1806_1807insGGG	ENSP00000261584.4:p.Gln602_Leu603insGly
ENST00000565038.1:c.87-1073_87-1072insGGG
ENST00000568219.5:c.921_922insGGG	ENSP00000454703.2:p.Gln307_Leu308insGly
NM_024675.3:c.1806_1807insGGG , LRG_308t1:c.1806_1807insGGG	NP_078951.2:p.Gln602_Leu603insGly
XM_011545946.1:c.1812_1813insGGG	XP_011544248.1:p.Gln604_Leu605insGly
XM_011545947.1:c.1812_1813insGGG	XP_011544249.1:p.Gln604_Leu605insGly
XM_011545948.1:c.921_922insGGG	XP_011544250.1:p.Gln307_Leu308insGly
XR_950851.1:n.2602_2603insGGG
XM_011545946.2:c.1812_1813insGGG	XP_011544248.1:p.Gln604_Leu605insGly
XM_011545947.2:c.1812_1813insGGG	XP_011544249.1:p.Gln604_Leu605insGly
XM_011545948.2:c.921_922insGGG	XP_011544250.1:p.Gln307_Leu308insGly
XM_017023671.1:c.1812_1813insGGG	XP_016879160.1:p.Gln604_Leu605insGly
XM_017023672.2:c.1806_1807insGGG	XP_016879161.1:p.Gln602_Leu603insGly
XM_017023673.2:c.1806_1807insGGG	XP_016879162.1:p.Gln602_Leu603insGly
NM_024675.4:c.1806_1807insGGG MANE Select	NP_078951.2:p.Gln602_Leu603insGly